中国有色金属学报
中國有色金屬學報
중국유색금속학보
THE CHINESE JOURNAL OF NONFERROUS METALS
2014年
6期
1671-1677
,共7页
李巧%曾虹燕%张治青%廖梦尘%黄清军%徐理华
李巧%曾虹燕%張治青%廖夢塵%黃清軍%徐理華
리교%증홍연%장치청%료몽진%황청군%서리화
镁铁水滑石%表面酸碱性%配位%电化学性能%结晶度
鎂鐵水滑石%錶麵痠堿性%配位%電化學性能%結晶度
미철수활석%표면산감성%배위%전화학성능%결정도
Mg-Fe hydrotalcite%urfaceacid-base property%coordination%electrochemical property%crystallinity
利用X射线衍射(XRD)、傅里叶变换红外光谱(FT-IR)、零电荷点pHPZC、循环伏安(CV)和电化学阻抗(EIS)等手段,研究镁铁水滑石(MgFe-LDHs)的表面化学性质,揭示其表面酸碱性与电化学性能的关系。结果表明:当Mg与Fe的摩尔比(n(Mg)/n(Fe))为3时MgFe-LDH (LDH-3)的结晶度最高,碱性最强,且远强于n(Mg)/n(Fe)为2的MgFe-LDH (LDH-2)和n(Mg)/n(Fe)为4的(LDH-4)的碱性。LDH-2的碱性略强于LDH-4的,但差异微小。层间CO32-与LDH层板金属离子主要形成单齿和双齿配位,其中,单齿配位体与强碱位点配位,形成Lewis碱位。表面碱性取决于Lewis强碱性位(CO32-单齿配位)的含量。用镁铁水滑石煅烧产物(MgFe-LDOs)修饰玻碳电极来研究其电化学性能。碱性越强(如LDO-3),其氧化还原可逆性及导电性能越好。
利用X射線衍射(XRD)、傅裏葉變換紅外光譜(FT-IR)、零電荷點pHPZC、循環伏安(CV)和電化學阻抗(EIS)等手段,研究鎂鐵水滑石(MgFe-LDHs)的錶麵化學性質,揭示其錶麵痠堿性與電化學性能的關繫。結果錶明:噹Mg與Fe的摩爾比(n(Mg)/n(Fe))為3時MgFe-LDH (LDH-3)的結晶度最高,堿性最彊,且遠彊于n(Mg)/n(Fe)為2的MgFe-LDH (LDH-2)和n(Mg)/n(Fe)為4的(LDH-4)的堿性。LDH-2的堿性略彊于LDH-4的,但差異微小。層間CO32-與LDH層闆金屬離子主要形成單齒和雙齒配位,其中,單齒配位體與彊堿位點配位,形成Lewis堿位。錶麵堿性取決于Lewis彊堿性位(CO32-單齒配位)的含量。用鎂鐵水滑石煅燒產物(MgFe-LDOs)脩飾玻碳電極來研究其電化學性能。堿性越彊(如LDO-3),其氧化還原可逆性及導電性能越好。
이용X사선연사(XRD)、부리협변환홍외광보(FT-IR)、령전하점pHPZC、순배복안(CV)화전화학조항(EIS)등수단,연구미철수활석(MgFe-LDHs)적표면화학성질,게시기표면산감성여전화학성능적관계。결과표명:당Mg여Fe적마이비(n(Mg)/n(Fe))위3시MgFe-LDH (LDH-3)적결정도최고,감성최강,차원강우n(Mg)/n(Fe)위2적MgFe-LDH (LDH-2)화n(Mg)/n(Fe)위4적(LDH-4)적감성。LDH-2적감성략강우LDH-4적,단차이미소。층간CO32-여LDH층판금속리자주요형성단치화쌍치배위,기중,단치배위체여강감위점배위,형성Lewis감위。표면감성취결우Lewis강감성위(CO32-단치배위)적함량。용미철수활석단소산물(MgFe-LDOs)수식파탄전겁래연구기전화학성능。감성월강(여LDO-3),기양화환원가역성급도전성능월호。
The surface chemical characteristics of the Mg-Fe hydrotalcites (MgFe-LDHs) were determined using X-ray diffractometry (XRD), Fourier transform-infrared spectrometer (FT-IR), point of zero charge (pHPZC), cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The relationship between the surfaceacid-base and electrochemical properties of the MgFe-LDHs was clarified. The results show that the MgFe-LDH with molar ratio of Mg to Fe (n(Mg)/n(Fe)) being 3 (LDH-3) has the highest crystallity structure with symmetrical crystals, indicating that the surface basicity of the LDH-3 is the strongest. And its basicity is much higher than those of ones with n(Mg)/n(Fe) of 2 (LDH-2) and 4 (LDH-4). The basicity of LDH-2 is slightly stronger than that of LDH-4. The monodentate and bidentate coordinations are formed by the interlayer CO32- anions coordinating with the metal ions in the brucite-like layers. The monodentate ligand coordinates with the strong basic sites, then Lewis basic sites form. The basicity depends on the content of Lewis basic sites. Mg-Fe hydrotalcite calcined samples (MgFe-LDOs) were used to modify glassy carbon electrode to study its electrochemical properties. The stronger the basicity (such as those of the LDO-3) is, the better the oxidation-reduction reversibility and conductivity are.